Classifications

• • C—CHEMISTRY; METALLURGY
  • C08—ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
  • C08K—Use of inorganic or non-macromolecular organic substances as compounding ingredients
  • C08K5/00—Use of organic ingredients
  • C08K5/54—Silicon-containing compounds
  • C08K5/544—Silicon-containing compounds containing nitrogen
  • C08K5/5477—Silicon-containing compounds containing nitrogen containing nitrogen in a heterocyclic ring
• • C—CHEMISTRY; METALLURGY
  • C08—ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
  • C08L—COMPOSITIONS OF MACROMOLECULAR COMPOUNDS
  • C08L83/00—Compositions of macromolecular compounds obtained by reactions forming in the main chain of the macromolecule a linkage containing silicon with or without sulfur, nitrogen, oxygen or carbon only; Compositions of derivatives of such polymers
  • C08L83/04—Polysiloxanes
• • C—CHEMISTRY; METALLURGY
  • C08—ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
  • C08K—Use of inorganic or non-macromolecular organic substances as compounding ingredients
  • C08K5/00—Use of organic ingredients
  • C08K5/54—Silicon-containing compounds
• • C—CHEMISTRY; METALLURGY
  • C08—ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
  • C08K—Use of inorganic or non-macromolecular organic substances as compounding ingredients
  • C08K5/00—Use of organic ingredients
  • C08K5/54—Silicon-containing compounds
  • C08K5/544—Silicon-containing compounds containing nitrogen
  • C08K5/5455—Silicon-containing compounds containing nitrogen containing at least one group
• • C—CHEMISTRY; METALLURGY
  • C08—ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
  • C08G—MACROMOLECULAR COMPOUNDS OBTAINED OTHERWISE THAN BY REACTIONS ONLY INVOLVING UNSATURATED CARBON-TO-CARBON BONDS
  • C08G77/00—Macromolecular compounds obtained by reactions forming a linkage containing silicon with or without sulfur, nitrogen, oxygen or carbon in the main chain of the macromolecule
  • C08G77/04—Polysiloxanes
  • C08G77/12—Polysiloxanes containing silicon bound to hydrogen
• • C—CHEMISTRY; METALLURGY
  • C08—ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
  • C08G—MACROMOLECULAR COMPOUNDS OBTAINED OTHERWISE THAN BY REACTIONS ONLY INVOLVING UNSATURATED CARBON-TO-CARBON BONDS
  • C08G77/00—Macromolecular compounds obtained by reactions forming a linkage containing silicon with or without sulfur, nitrogen, oxygen or carbon in the main chain of the macromolecule
  • C08G77/04—Polysiloxanes
  • C08G77/14—Polysiloxanes containing silicon bound to oxygen-containing groups
  • C08G77/18—Polysiloxanes containing silicon bound to oxygen-containing groups to alkoxy or aryloxy groups

Definitions

• Organopolysiloxane compositions which can be crosslinked with the elimination of alcohols to give elastomers
• the invention relates to organopolysiloxane compositions which are storable with the exclusion of moisture and which cure under the influence of moisture at room temperature with the elimination of alcohols to give elastomers and which are distinguished by a particularly high storage stability.
• organopolysiloxanes is intended to encompass dimeric, oligomeric and polymeric siloxanes.
• RTV-1 alkoxy compositions Organopolysiloxane compositions which can be stored in the absence of moisture and which crosslink under the ingress of moisture at room temperature with the elimination of alcohols, so-called RTV-1 alkoxy compositions, have long been known. They essentially consist of silicone polymer terminated with organyloxy groups, crosslinking agents with at least three hydrolyzable groups, catalyst and, if appropriate, additives. The advantage of these RTV-1 alkoxy systems is that they only release odorless, neutral, environmentally compatible cleavage products - namely alcohols - during the crosslinking process.
• RTV-1 alkoxy masses A major disadvantage of the RTV-1 alkoxy masses is the reduced storage stability compared to the corresponding vinegar, oxime and amine systems. This means that the RTV Although 1-alkoxy mass cures to an elastomer in the desired manner after production, these curing properties are usually lost when the compositions are stored in the absence of air. After a longer storage period, it is therefore generally observed that curing to elastomers takes longer, and their mechanical properties are significantly poorer than those of the initial elastomers. In the worst case, curing to elastomers can not occur completely after storage.
• the cause of this change in the hardening over time is frequently the equilibration of polymer chains with free alcohol dissolved in the mass, with catalysis by the organometallic condensation catalyst, polymer ends being generated with an alkoxy group which are necessary for further reaction to form a network under the an ⁇ application conditions (room temperature) are too inert. So there is no networking.
• the alcohol for this undesired equilibration reaction arises from the reaction of the alkoxy crosslinking agent with water and other OH groups, such as, for example, silanol groups, which are inevitable in the preparation of the RTV-1 alkoxy compositions via the polymer, the filler and any other additives and the method of manufacture (reaction vessel, manufacture in the atmosphere) get into the mass.
• the present invention relates to organopolysiloxane compositions which are storable with the exclusion of moisture and can be crosslinked with the ingress of moisture at room temperature with the elimination of alcohols to give elastomers
• (C) condensation catalysts characterized in that they have at least one
• (D) contain compound selected from (D a ) compounds of the general formula
• R 4 is a divalent hydrocarbon radical with 1 to 16 carbon atoms optionally substituted with halogen atoms, amino groups, ether groups or ester groups,
• R 9 may be the same or different and SiC-bonded monovalent hydrocarbon radicals having 1 to 12 carbon atoms, which are optionally substituted with halogen atoms, amino groups, ether groups, ester groups, epoxy groups, mercapto groups, cyano groups or (poly) glycol radicals, the latter consisting of oxyethylene and / or oxypropylene units are constructed, as well as organosiloxy and c is 0 or an integer from 1 to 20, and
• R 10 may be the same or different and means hydrogen atom and hydrocarbon radicals having 1 to 8 carbon atoms which are optionally substituted by halogen atoms, amino groups, ether groups or ester groups.
• compositions according to the invention can be stable or flowable.
• the polydiorganosiloxanes used according to the invention with at least two organyloxy radicals on each end group are preferably those of the general formula
• R 1 can be the same or different and is hydrogen or has the meaning given for R,
• R 2 may be the same or different and represents a hydrocarbon radical with 1 to 18 carbon atoms which may be substituted by amino, ester, ether, keto or halogen groups and which may be interrupted by oxygen atoms, and n is an integer from 10 to 10,000, preferably 100 to 3,000, particularly preferably 400 to 2,000.
• hydrocarbon radicals R and R 1 are alkyl radicals, such as the methyl, ethyl, n-propyl, iso-propyl, 1-n-butyl, 2-n-butyl, iso-butyl, tert .-Butyl, n-pentyl, iso-pentyl, neo-pentyl, tert-pentyl; Hexyl radicals, such as the n-hexyl radical; Heptyl residues, such as the n-heptyl residue; Octyl radicals, such as the n-octyl radical and iso-octyl radicals, such as the 2,2,4-trimethylpentyl radical; Nonyl radicals, such as the n-nonyl radical; Decyl radicals, such as the n-decyl radical; Dodecyl residues, such as the n-do-decyl residue; Octadecl
• substituted hydrocarbon radicals R and R 1 are halogenated radicals, such as the 3-chloropropyl radical, the 3,3,3-trifluoropropyl radical, chlorophenyl radicals, hexafluoropropyl radicals, such as the 1-trifluoromethyl 1--2,2,2-trifluoroethyl radical; the 2- (perfluorohexyl) ethyl radical, the 1,1,2,2-tetrafluoroethyloxypropyl radical, the l-trifluoromethyl-2,2,2-trifluoroethyloxypropyl radical, the perfluoroisopropyloxyethyl radical, the perfluoroisopropyloxypropyl radical; residues substituted by amino groups, such as the N- (2-aminoethyl) -3-aminopropyl residue, the 3-aminopropyl residue and the 3- (cyclohexylamino) propyl residue; ether functional radicals,
• Preferred radicals R are unsubstituted hydrocarbon radicals having 1 to 10 carbon atoms and hydrocarbon radicals having 1 to 10 carbon atoms substituted by amino groups or by fluorine radicals, the methyl radical being particularly preferred.
• the radical R 1 is preferably a hydrogen atom, unsubstituted hydrocarbon radicals having 1 to 10 carbon atoms and hydrocarbon radicals having 1 to 10 carbon atoms substituted by amino, mercapto, morpholino, glycidoxy, acryloxy or methacryloxy groups.
• the R 1 radical is particularly preferably an alkyl radical and an alkenyl radical having 1 to 4 carbon atoms, in particular the methyl, ethyl and vinyl radicals, and optionally linked to the silicon atom via alkylene radicals having 2 to 6 carbon atoms substituted amino and glycidoxy groups.
• alkylene radicals R 1 are the hydrocarbon radicals specified for R.
• substituted hydrocarbon radicals R 1 are the 3- (2-aminoethylamino) propyl radical, the 3- (cyclohexylamino) propyl radical, the 3- (glycidoxy) propyl radical, 3- (N, N-diethyl-2-aminoethylamino) propyl radical, 3- (butylamino) propyl and 3- (3-methoxypropylamino) propyl.
• the radical R 2 is preferably alkyl radicals having 1 to 8 carbon atoms, which can be substituted by methoxy or ethoxy groups, methyl or ethyl radicals being particularly preferred.
• alkyl radicals R 2 are the examples of alkyl radicals given above for R.
• the average value for the number n in formula (II) is preferably chosen so that the organopolysiloxane of the formula (II) has a viscosity of 1,000 to 1,000,000 mm 2 / s, particularly preferably 5,000 to 500,000 mm 2 / s, measured at a temperature of 25 ° C.
• Examples of the polydiorganosiloxanes used in the compositions according to the invention with at least two organyloxy radicals on each end group (A) are (MeO) 2 MeSiO [SiMe2 O] 200 - 2 000 s i Me (° Me) 2 / (EtO) 2 MeSiO [SiMe2 0] 20 o-2000 s iMe (OEt) 2, (MeO) 2 ViSi ⁇ [SiMe 2 O] 200 -2000 s i vi (OMe) 2, (EtO) 2 ViSi ⁇ [SiMe 2 0] 20 0-2 00 0 s iVi (OEt) 2, (MeO) 2 CapSiO [SiMe 2 0] 2 oo-2 00 0 siCa P ( 0Me ) 2 / ( Me O) 2 Bap S i O [S iMe 2 0 ] 20 o-2000 siBa P (
• the organopolysiloxane (A) used according to the invention can be a single type or a mixture of at least two types of such organopolysiloxanes.
• the polydiorganosiloxanes used in the compositions according to the invention with at least two organyloxy radicals on each end group are commercially available products or can be prepared by processes known in silicon chemistry, for example by reacting ⁇ , ⁇ -dihydroxypolyorganosiloxanes with the corresponding organyloxysilanes.
• organyloxy-functional crosslinking agents (B) which may be used can be any known organyloxy crosslinking agents such as silanes or siloxanes with at least three organyloxy groups and cyclic silanes according to DE-A 36 24 206 (Wacker-Chemie GmbH; on February 11, 1988) or the corresponding US-A 4,801,673 of the formula
• R 6 represents a divalent hydrocarbon radical
• R 7 can be the same or different and has a meaning given for R 2 and
• R8 represents hydrogen atom, an alkyl or an aminoalkyl radical.
• organyloxy crosslinking agents (B) optionally used in the compositions according to the invention are preferably organosilicon compounds of the formula
• R 2 can be the same or different and has one of the meanings given above,
• R 3 has the meaning given above for R 1 or represents a hydrocarbon radical substituted by the radical -SiR 1 j D (OR 2 ) ⁇ -b, with R 1 and R 2 being the same as the abovementioned meaning and b being 0.1 , 2 or 3 and m is 0 or 1, and their partial hydrolyzates.
• the partial hydrolyzates can be partial homohydrolysates, i.e. Partial hydrolysates of a type of organosilicon compound of formula (IV) as well as partial cohydrolysates, i.e. Partial hydrolysates of at least two different types of organosilicon compounds of the formula (IV).
• crosslinking agents (B) used in the compositions according to the invention are partial hydrolysates of organosilicon compounds of the formula (IV), those with up to 6 silicon atoms are preferred.
• radical R 3 are the examples mentioned above for radical R 1 and also hydrocarbon radicals with 1 to 6 carbon atoms substituted with radicals -SiR 1 j D (OR 2 ) 3-b, where b is 0 or 1 and R 2 is has the above meaning.
• R 3 are the radicals which are mentioned with preference for R 1 and also hydrocarbon radicals having 1 to 6 carbon atoms substituted by radicals -SiR j ⁇ OR 2 ) 3_t, where b is 0 or 1 and R 2 has the abovementioned meaning.
• radicals R 3 are the radicals which are particularly preferred for R 1 and hydrocarbon radicals having 2 carbon atoms and substituted with radicals -Si (OR 2 ) 3, where R 2 is ethyl or methyl radical.
• crosslinking agents (B) optionally used in the compositions according to the invention are particularly preferably tetramethoxysilane, tetraethoxysilane, methyltrimethoxysilane, methyltriethoxy ⁇ ilane, vinyltrimethoxysilane, vinyltriethoxy ⁇ ilane, phenyltrimethoxysiloxysilane, phenyltriloxysilane, phenyltriloxysilane, phenyltriloxysilane, Cyanopropyltrimethoxysilane, 3-cyanopropyltriethoxysilane, 3- (2-aminoethylamino) propyltrimethoxysilane, 3- (2-aminoethylamino) propyltriethoxysilane, 3- (N, N-diethyl-2-aminoethylamino) propyltrimethoxysilane, 3- (N, Diethyl-2-aminoeth
• the crosslinker (B) optionally used according to the invention can be a single type or a single type Act a mixture of at least two types of such organyloxy crosslinkers.
• crosslinking agents (B) used in the compositions according to the invention are commercially available products or can be prepared by processes known in silicon chemistry.
• compositions according to the invention contain crosslinking agents (B) in amounts of preferably 0 to 50 parts by weight, particularly preferably 0.1 to 20 parts by weight, in particular 0.5 to 10 parts by weight, in each case based on 100 parts by weight of organopolysiloxane (A).
• compositions according to the invention can contain any condensation catalysts (C) which have hitherto been available in compositions which can be stored under exclusion of water and which crosslink to form elastomers when water is added at room temperature.
• condensation catalysts such as butyl titanates and organic tin compounds, such as di-n-butyltin diacetate, di-n-butyltin dilaurate and reaction products of at least two per molecule which are bonded to silicon via oxygen, optionally substituted by an alkoxy group, monovalent hydrocarbon radicals as hydrolyzable groups containing silane or its oligomer with diorganotin diacylate, in these reaction products all valences of the tin atoms by oxygen atoms of the grouping
• condensation catalysts (C) are organometallic condensation catalysts, in particular derivatives of titanium, aluminum, tin, and calcium and zinc, dialkyltin compounds and zinc dicarboxylates being particularly preferred.
• organometallic condensation catalysts examples include the dialkyldi ( ⁇ -dike-to) stannates described in US Pat. No. 4,517,337 (General Electric Co .; issued May 14, 1985), dialkyltin dicarboxylates, calcium and zinc dicarboxylates and butyltitanium chelate compounds.
• organometallic condensation catalysts are dibutyltin diacetate, dibutyltin dilaurate, dibutyltin di (2-ethylhexanoate) and zinc di (2-ethylhexanoate).
• the condensation catalysts (C) optionally used in the compositions according to the invention can be a single type or a mixture of at least two types of such condensation catalysts.
• the masses according to the invention contain condensation catalyst (C) in amounts of preferably 0 to 10 parts by weight, particularly preferably 0.01 to 5 parts by weight, in particular 0.1 to 4 parts by weight, in each case based on 100 parts by weight of organopolysiloxane (A).
• radicals R 4 are methylene, 1,2-ethylene, 1,3-propylene, 1,4-butylene, methyl-1,2-ethylene, 1-methyl-1,3-propylene , 2-methyl-l, 3-propylene, 2, 2-dimethyl-l, 3-propylene and 2-ethyl-l, 3-propylene.
• R 4 preferably denotes a radical - (CR 5 2 ) y-, where R 5 can be the same or different and hydrogen atom or Is a hydrocarbon radical having 1 to 4 carbon atoms and y is an integer from 1 to 8, preferably 2, 3 or 4, R 4 particularly preferably meaning 1,2-ethylene radical and 1,3-propylene radical.
• radical R 5 is particularly preferably a hydrogen atom or the methyl radical, in particular a hydrogen atom.
• radical R 5 are the examples of hydrocarbon radicals with 1 to 4 carbon atoms given for R above.
• R 9 are the examples given for R for optionally substituted hydrocarbon radicals having 1 to 12 carbon atoms and organosiloxy radicals, such as the trimethylsiloxy radical, the triethylsiloxy radical, the dimethylphenylsiloxy radical, the (CH 3 ) 3 SiO- [Si (CH 3 ) 2 0 ] 3 residue and the (CH 3 ) 3 SiO- [Si (CH 3 ) 2 0] 4 residue.
• organosiloxy radicals such as the trimethylsiloxy radical, the triethylsiloxy radical, the dimethylphenylsiloxy radical, the (CH 3 ) 3 SiO- [Si (CH 3 ) 2 0 ] 3 residue and the (CH 3 ) 3 SiO- [Si (CH 3 ) 2 0] 4 residue.
• R 9 is preferably a hydrocarbon radical having 1 to 12 carbon atoms, particularly preferably the methyl radical.
• the value for c is preferably 0 or an integer from 1 to 10, particularly preferably 0 or an integer from 1 to 4, in particular 0.
• R 10 are the examples given for R for optionally substituted hydrocarbon radicals having 1 to 8 carbon atoms.
• the radical R 10 is preferably a hydrogen atom and hydrocarbon radicals having 1 to 6 carbon atoms, particularly preferably a hydrogen atom.
• Examples of compounds (D a ) according to formula (Ia) with Z equal to -0- are optionally substituted 3-trimethylsilyl-1,3-oxazolidin-2-ones, such as those of the formula
• Me means methyl radical
• Me means methyl radical
• Examples of compounds (D c ) according to formula (Ic) are optionally substituted 1,4-bis (trimethylsilyl) piperazines, such as those of the formula
• Me means methyl radical
• O-silylated, optionally substituted hydroxypyrimidines are compounds of the formula
• a and R 10 have one of the meanings mentioned above, such as bis ( ⁇ -trimethylsilyl) uracil, bis (O-trimethylsilyl) thymine and tris (O-trimethylsilyl) barbituric acid
• Me means methyl radical
• Examples of compounds (D e ) according to formula (le) are optionally substituted N, N ⁇ - bis (trimethylsilyl) ureylenes, such as, for example, those of the formulas
• Me means methyl radical
• silylated, optionally substituted hydroxy purines are tetrakis (trimethylsilyl) uric acid and compounds of the formula AO-C
• radicals A in this molecule preferably have the same meaning.
• the compounds (D a ) to (Df) are commercially available products or can be prepared by processes described in the literature and common in silicon chemistry.
• the component (D) used in the compositions according to the invention can be a single type or a mixture of at least two types of such compounds.
• compositions according to the invention contain compound (D) in amounts of preferably 0.1 to 10 parts by weight, particularly preferably 0.5 to 6 parts by weight, in particular 0.5 to 5 parts by weight, in each case based on 100 parts by weight of organopolysiloxane (A).
• compositions according to the invention can now contain further substances, such as plasticizers (E), fillers (F), adhesion promoters (G) and additives (H) , the additional substances (E) to (H) being the same as those which have hitherto been used in compositions which can be crosslinked by splitting off alcohols.
• plasticizers E
• fillers F
• adhesion promoters G
• additives H
• the additional substances (E) to (H) being the same as those which have hitherto been used in compositions which can be crosslinked by splitting off alcohols.
• plasticizers (E) are liquid dimethylpolysiloxanes which are blocked by trimethylsiloxy groups at room temperature and high-boiling hydrocarbons, such as paraffin oils.
• compositions according to the invention contain plasticizers (E) in amounts of preferably 0 to 300 parts by weight, particularly preferably 10 to 200 parts by weight, in particular 20 to 100 parts by weight, in each case based on 100 parts by weight of organopolysiloxane (A).
• fillers (F) are non-reinforcing fillers, that is fillers with a BET surface area of up to 50 m 2 / g, such as quartz, diatomaceous earth, calcium silicate, zirconium silicate, zeolites, metal oxide powders, such as aluminum, titanium, iron or Zinc oxides or their mixed oxides, barium sulfate, calcium carbonate, gypsum, silicon nitride, silicon carbide, boron nitride, glass and plastic powder, such as polyacrylonitrile powder; reinforcing fillers, ie fillers with a BET surface area of more than 50 m 2 / g, such as pyrogenic silica, precipitated silica, carbon black, such as furnace black and acetylene black and silicon-aluminum mixed oxides of large BET surface area; fibrous fillers, such as Asbestos and plastic fibers.
• the fillers mentioned can be hydrophobized, for example by treatment with organos
• compositions according to the invention contain fillers (F) in amounts of preferably 0 to 300 parts by weight, particularly preferably 1 to 200 parts by weight, in particular 5 to 200 parts by weight, in each case based on 100 parts by weight of organopolysiloxane (A).
• adhesion promoters (G) used in the organopolysiloxane compositions according to the invention are silanes and organopolysiloxanes with functional groups, such as, for example, those with aminoalkyl, glycidoxypropyl or methacryloxypropyl radicals and tetraalkoxysilanes.
• functional groups such as, for example, those with aminoalkyl, glycidoxypropyl or methacryloxypropyl radicals and tetraalkoxysilanes.
• siloxane (A) or crosslinker (B) already has the functional groups mentioned, it is not necessary to add an adhesion promoter.
• compositions according to the invention contain adhesion promoters (G) in amounts of preferably 0 to 50 parts by weight, particularly preferably 1 to 20 parts by weight, in particular 1 to 10 parts by weight, in each case based on 100 parts by weight of organopolysiloxane (A).
• additives (H) are pigments, dyes, fragrances, fungicides, oxidation inhibitors, agents for influencing the electrical properties, such as conductive carbon black, flame-retarding agents, light stabilizers and agents for prolonging the skin formation time, such as silanes with a silicate. bound mercaptoalkyl radical, cell-producing agents, for example azodicarbonamide, heat stabilizers and thixotropic agents.
• the compositions according to the invention contain additives (H) in amounts of preferably 0 to 100 parts by weight, particularly preferably 0 to 30 parts by weight, in particular 0 to 10 parts by weight, in each case based on 100 parts by weight of organopolysiloxane (A).
• the individual constituents (E), (F), (G) and (H) of the organopolysiloxane compositions according to the invention which can be crosslinked by splitting off alcohols can each be a type of such constituent or a mixture of at least two types of such Trade components.
• compositions according to the invention are preferably those which
• compositions according to the invention are particularly preferably those which consist of
• compositions according to the invention all constituents of the particular composition can be mixed together in any order. This mixing can take place at room temperature and the pressure of the surrounding atmosphere, ie about 900 to 1100 hPa. If desired, this mixing can also take place at higher temperatures, for example at temperatures in the range from 35 ° C. to 135 ° C.
• compositions according to the invention must be carried out under essentially water-free conditions, since otherwise the compositions may harden prematurely.
• the crosslinking can also be carried out at temperatures higher or lower than room temperature, e.g. at -5 "to 10" C or at 30 ° to 50 ° C.
• the organopolysiloxane compositions which can be crosslinked with the elimination of alcohols to give elastomers have the advantage that they are distinguished by a very high storage stability and a high crosslinking rate.
• the compositions according to the invention show constant vulcanization behavior at all times when stored for at least 18 months at room temperature.
• compositions according to the invention have the advantage that the compounds (D a ) to (Df) react with OH groups, in particular with alcohol and / or water and / or Si-OH groups, even at room temperature.
• Compounds with OH groups in RTV alkoxy compositions are mainly water, which is introduced into the composition with the formulation components such as the polysiloxane or the fillers. holes that form during the end blocking of the OH polymers and the reaction of Si-OH groups or water with crosslinking agents, and Si-OH groups on polysiloxanes and especially on the silica optionally used as filler.
• no ecologically questionable or odor-causing, volatile fission products are released.
• compositions according to the invention are easily accessible synthetically and are therefore economical to produce.
• compositions according to the invention or those produced according to the invention can be used for all purposes for which organopolysiloxane compositions which can be stored with the exclusion of water and which crosslink to form elastomers when water is added at room temperature can be used.
• compositions according to the invention or those produced according to the invention are therefore outstandingly suitable, for example, as sealing compositions for joints, including vertically running joints, and similar empty spaces, e.g. 10 to 40 mm clear width, e.g. of buildings, land, water and air vehicles, or as adhesives or cementing compounds, e.g. in window construction or in the production of aquariums or showcases, as well as e.g. for the production of protective coatings, including surfaces exposed to the constant action of fresh water or sea water, or coatings which prevent sliding, or of rubber-elastic molded bodies, and for the insulation of electrical or electronic devices.
• sealing compositions for joints including vertically running joints, and similar empty spaces, e.g. 10 to 40 mm clear width, e.g. of buildings, land, water and air vehicles, or as adhesives or cementing compounds, e.g. in window construction or in the production of aquariums or showcases, as well as e.g. for the production of protective coatings, including surfaces exposed to the constant action of fresh water
• Shore A hardness is determined according to DIN (German Industry Standard).
• u-bis (dimethoxymethyl) polydimethylsiloxane with a viscosity of 80,000 mm 2 / s are added 28 g of an ⁇ , u-bis (trimethylsiloxy) polydimethylsiloxane with a viscosity of 0.1 mm 2 / s, 1.6 g Methyltrimethoxysilane and 1 g of 3-aminopropyltrieth ⁇ oxysilane (commercially available under the name "Silan GF 93" from Wacker-Chemie GmbH) mixed.
• the mass produced in this way is filled airtight into tubes and stored at 50 ° C.
• Example 1 The procedure described in Example 1 is repeated with the modification that instead of the 4 g of 3-trimethylsilyl-2-oxazolidinone, 4 g of 1-trimethylsilyl-1,2,4-triazole (commercially available from ABCR, D-Karl ⁇ ruhe) be stirred into the mass.
• 4 g of 1-trimethylsilyl-1,2,4-triazole commercially available from ABCR, D-Karl ⁇ ruhe
• the mass produced in this way is filled airtight into tubes and stored at 50 ° C.
• Example 3 Immediately after the production and after 2, 4, 8 and 12 weeks of storage, the skin formation time (time to form a dry surface of the caterpillar) and the Shore A hardness using 2 mm are determined using caterpillars as described in Example 1 thick foils determined. The results are summarized in Table 1.
• Example 3 Immediately after the production and after 2, 4, 8 and 12 weeks of storage, the skin formation time (time to form a dry surface of the caterpillar) and the Shore A hardness using 2 mm are determined using caterpillars as described in Example 1 thick foils determined. The results are summarized in Table 1. Example 3
• Example 1 The procedure described in Example 1 is repeated with the modification that instead of the 4 g of 3-trimethylsilyl-2-oxazolidinone, 4 g of bis-N, N '- (trimethylsilyl) piperazine (commercially available from ABCR, D- Düsseldorf) are stirred into the mass.
• 4 g of bis-N, N '- (trimethylsilyl) piperazine commercially available from ABCR, D- Düsseldorf
• the mass produced in this way is filled airtight into tubes and stored at 50 ° C.
• Example 1 The procedure described in Example 1 is repeated with the modification that instead of the 4 g of 3-trimethylsilyl-2-oxazolidinone, 4 g of bis (0-trimethylsilyl) uracil (commercially available from ABCR, D-Karlsruhe) are incorporated into the Mass are stirred.
• 4 g of bis (0-trimethylsilyl) uracil commercially available from ABCR, D-Karlsruhe
• the mass produced in this way is filled airtight into tubes and stored at 50 ° C.
• Example 5 Immediately after the manufacture and after 2, 4, 8 and 12 weeks of storage, the skin formation time (time until a dry surface of the bead is formed) and the Shore A hardness are determined using 2 mm thick foils using beads. The results are summarized in Table 1.
• Example 5 Immediately after the manufacture and after 2, 4, 8 and 12 weeks of storage, the skin formation time (time until a dry surface of the bead is formed) and the Shore A hardness are determined using 2 mm thick foils using beads. The results are summarized in Table 1. Example 5
• Example 1 The procedure described in Example 1 is repeated with the modification that instead of the 4 g of 3-trimethylsilyl-2-oxazolidinone, 4 g of N, N'-bis (trimethylsilyl) urea (commercially available under the name "Silan BSU” from Wacker- Chemie GmbH) are stirred into the mass.
• 4 g of N, N'-bis (trimethylsilyl) urea commercially available under the name "Silan BSU” from Wacker- Chemie GmbH
• the mass produced in this way is filled airtight into tubes and stored at 50 ° C.
• Example 1 The procedure described in Example 1 is repeated with the modification that instead of the 4 g of 3-trimethylsilyl-2-oxazolidinone, 4 g of tetrakis (trimethylsilyl) uric acid, the preparation of which is described above under A), are stirred into the mass.
• the mass produced in this way is filled airtight into tubes and stored at 50 ° C.
• Example 1 The procedure described in Example 1 is repeated with the modification that instead of the 4 g of 3-trimethylsilyl-2-oxazolidinone, 4 g of N, N ⁇ - bis (trimethylsilyl) -2-imidazolidinone, the preparation of which is described above under A), in the mass are stirred in.
• the mass produced in this way is filled airtight into tubes and stored at 50 ° C.
• Example 1 The procedure described in Example 1 is repeated with the modification that instead of the 4 g of 3-trimethylsilyl-2-oxazolidinone, 4 g of bis (O-trimethylsilyl) thymine (commercially available from ABCR, D-Karlsruhe) are added to the mass be stirred.
• 4 g of bis (O-trimethylsilyl) thymine commercially available from ABCR, D-Karlsruhe
• the mass produced in this way is filled airtight into tubes and stored at 50 ° C.
• Example 1 The procedure described in Example 1 is repeated with the modification that instead of the 4 g of 3-trimethylsilyl-2-oxazolidinone, 4 g of N, N * bis (trimethylsilyl) tetrahydropyrimidinone, the preparation of which is described above under A), in the Mass to be stirred.
• the mass produced in this way is filled airtight into tubes and stored at 50 ° C.
• the skin formation time time until a dry surface of the bead is formed
• the Shore A hardness are determined using 2 mm thick foils using beads. The results are summarized in Table 1.
• Example 1 The procedure described in Example 1 is repeated with the modification that instead of the 4 g of 3-trimethylsilyl-2-oxazolidinone, 4 g of N, N X -bis (trimethylsilyl) -N, N x -dimethylurea, the preparation of which under A ) is stirred into the mass.
• the mass produced in this way is filled airtight into tubes and stored at 50 ° C.
• the skin formation time time until a dry surface of the bead is formed
• the Shore A hardness are determined using 2 mm thick foils using beads. The results are summarized in Table 1.
• HBZ skin formation time in minutes
• Sh-A Shore A hardness
• Example 1 The procedure described in Example 1 is repeated with the modification that instead of the 4 g of 3-trimethylsilyl-2-oxazolidinone 4 g of N, N-bis (trimethylsilyl) methylamine (commercially available from Fluka, CH-Buchs) in the Mass are stirred.
• the mass produced in this way is filled airtight into tubes and stored at 50 ° C.
• Example 1 The procedure described in Example 1 is repeated with the modification that instead of the 4 g of 3-trimethylsilyl-2-oxazolidinone, 4 g of N-trimethylsilylmorpholine (commercially available from ABCR, D-Karlsruhe) are stirred into the mass.
• 4 g of N-trimethylsilylmorpholine commercially available from ABCR, D-Karlsruhe
• the mass produced in this way is filled airtight into tubes and stored at 50 ° C.
• Example 1 The procedure described in Example 1 is repeated with the modification that instead of the 4 g of 3-trimethylsilyl-2-oxazolidinone, 4 g of N, 0-bis (trimethylsilyl) hydroxylamine (commercially available from ABCR, D-Karlsruhe) be stirred into the mass.
• 4 g of N, 0-bis (trimethylsilyl) hydroxylamine commercially available from ABCR, D-Karlsruhe
• the mass produced in this way is filled airtight into tubes and stored at 50 ° C.
• Example 1 The procedure described in Example 1 is repeated with the modification that instead of the 4 g of 3-trimethylsilyl-2-oxazolidinone, 4 g of 2- (trimethylsilyloxy) furan (commercially available from ABCR, D-Karlsruhe) are added to the mass be stirred.
• 4 g of 2- (trimethylsilyloxy) furan commercially available from ABCR, D-Karlsruhe
• the mass produced in this way is filled airtight into tubes and stored at 50 ° C.
• Example 1 The procedure described in Example 1 is repeated with the modification that instead of the 4 g of 3-trimethylsilyl-2-oxazolidinone, 4 g of trimethylsilylpyrrolidine (commercially available from ABCR, D-Karlsruhe) are stirred into the mass.
• 4 g of trimethylsilylpyrrolidine commercially available from ABCR, D-Karlsruhe
• the mass produced in this way is filled airtight into tubes and stored at 50 ° C.
• Example 1 The procedure described in Example 1 is repeated with the modification that instead of the 4 g of 3-trimethylsilyl-2-oxazolidinone, 4 g of trimethylsilylacetonitrile (commercially available from ABCR, D-Karlsruhe) are stirred into the mass.
• 4 g of trimethylsilylacetonitrile commercially available from ABCR, D-Karlsruhe
• the mass produced in this way is filled airtight into tubes and stored at 50 ° C.
• Example 1 The procedure described in Example 1 is repeated with the modification that instead of the 4 g of 3-trimethylsilyl-2-oxazolidinone, 4 g of bis (trimethylsilyl) carbodiimide (commercially available from ABCR, D-Karlsruhe) are stirred into the mass.
• 4 g of bis (trimethylsilyl) carbodiimide commercially available from ABCR, D-Karlsruhe
• the mass produced in this way is filled airtight into tubes and stored at 50 ° C.
• Example 1 The procedure described in Example 1 is repeated with the modification that instead of the 4 g of 3-trimethylsilyl-2-oxazolidinone, 4 g of trimethylsilylpiperidine (commercially available from ABCR, D-Karlsruhe) are stirred into the mass.
• 4 g of trimethylsilylpiperidine commercially available from ABCR, D-Karlsruhe
• the mass produced in this way is filled airtight into tubes and stored at 50 ° C.
• Example 1 The procedure described in Example 1 is repeated with the modification that instead of the 4 g of 3-trimethylsilyl-2-oxazolidinone, 4 g of tris (trimethylsilyl) ketenimine (commercially available from ABCR, D-Karlsruhe) are stirred into the mass.
• 4 g of tris (trimethylsilyl) ketenimine commercially available from ABCR, D-Karlsruhe
• the mass produced in this way is filled airtight into tubes and stored at 50 ° C.
• Example 1 The procedure described in Example 1 is repeated with the modification that instead of the 4 g of 3-trimethylsilyl-2-oxazolidinone, 4 g of tris (trimethylsilyl) phosphate (commercially available from ABCR, D-Karlsruhe) are stirred into the mass.
• 4 g of tris (trimethylsilyl) phosphate commercially available from ABCR, D-Karlsruhe
• the mass produced in this way is filled airtight into tubes and stored at 50 ° C.
• the skin formation time is determined using caterpillars (Time until a dry surface of the caterpillar is formed) and the Shore A hardness is determined using 2 mm thick foils. The results are summarized in Table 2.
• Example 1 The procedure described in Example 1 is repeated with the modification that instead of the 4 g of 3-trimethylsilyl-2-oxazolidinone, 4 g of trimethylsilyl methacrylate (commercially available from ABCR, D-Karlsruhe) are stirred into the mass.
• 4 g of trimethylsilyl methacrylate commercially available from ABCR, D-Karlsruhe
• the mass produced in this way is filled airtight into tubes and stored at 50 ° C.
• Example 1 The procedure described in Example 1 is repeated with the modification that instead of the 4 g of 3-trimethylsilyl-2-oxazolidinone, 4 g of 2-trimethylsilylethanol (commercially available from ABCR, D-Karlsruhe) are stirred into the mass.
• 4 g of 2-trimethylsilylethanol commercially available from ABCR, D-Karlsruhe
• the mass produced in this way is filled airtight into tubes and stored at 50'C.
• the skin formation time time until a dry surface of the bead is formed
• the Shore A hardness are determined using 2 mm thick foils using beads. The results are summarized in Table 2.
• Example 2 The procedure described in Example 1 is repeated with the modification that instead of the 4 g of 3-trimethyl-silyl-2-oxazolidinone, 4 g of bis (trimethylsilyl) acetamide (commercially available from Wacker-Chemie GmbH under the name "Silan BSA”) be stirred into the mass.
• 4 g of bis (trimethylsilyl) acetamide commercially available from Wacker-Chemie GmbH under the name "Silan BSA
• the mass produced in this way is filled airtight into tubes and stored at 50 ° C.
• Example 1 The procedure described in Example 1 is repeated with the modification that instead of the 4 g of 3-trimethylsilyl-2-oxazolidinone, 4 g of ethyltrimethylsilylacetate (commercially available from ABCR, D-Karlsruhe) are stirred into the mass.
• 4 g of ethyltrimethylsilylacetate commercially available from ABCR, D-Karlsruhe
• the mass produced in this way is filled airtight into tubes and stored at 50 ° C.
• the skin formation time time until a dry surface of the bead is formed
• the Shore A hardness are determined using 2 mm thick foils using beads. The results are summarized in Table 2.
• Example 1 The procedure described in Example 1 is repeated with the modification that instead of the 4 g of 3-trimethylsilyl-2-oxazolidinone, 4 g of N-methyl-N-trimethylsilylacetamide (commercially available from Fluka, CH-Buchs) are added to the mass ⁇ be stirred.
• 4 g of N-methyl-N-trimethylsilylacetamide commercially available from Fluka, CH-Buchs
• the mass produced in this way is filled airtight into tubes and stored at 50 ° C.
• Example 1 The procedure described in Example 1 is repeated with the modification that instead of the 4 g of 3-trimethylsilyl-2-oxazolidinone, 4 g (isopropenyloxy) trimethylsilane (commercially available from ABCR, D-Karlsruhe) are stirred into the mass.
• 4 g isopropenyloxy trimethylsilane (commercially available from ABCR, D-Karlsruhe) are stirred into the mass.
• the mass produced in this way is filled airtight into tubes and stored at 50 ° C.
• Sh-A Shore A hardness
• k.V. no vulcanization within 7 days

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• 1995
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